2,5-Dioxopyrrolidin-1-yl 6-(2-(tert-butoxycarbonyl)hydrazinyl)nicotinate

95%

Reagent Code: #176009
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CAS Number 133081-26-2

science Other reagents with same CAS 133081-26-2

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scatter_plot Molecular Information
Weight 350.33 g/mol
Formula C₁₅H₁₈N₄O₆
badge Registry Numbers
MDL Number MFCD03788694
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, stored away from light

description Product Description

Used as an activated ester in bioconjugation reactions, particularly in the modification of peptides and proteins. It reacts efficiently with primary amines under mild conditions to form stable amide bonds, making it valuable in the synthesis of bioconjugates for pharmaceutical and diagnostic applications. Commonly employed in the preparation of antibody-drug conjugates (ADCs) and labeled biomolecules due to its selective reactivity and compatibility with aqueous buffers. The presence of a protected hydrazine group allows for orthogonal functionalization, enabling sequential conjugation strategies in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,570.00
inventory 250mg
10-20 days ฿5,500.00
inventory 1g
10-20 days ฿11,100.00

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2,5-Dioxopyrrolidin-1-yl 6-(2-(tert-butoxycarbonyl)hydrazinyl)nicotinate
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Used as an activated ester in bioconjugation reactions, particularly in the modification of peptides and proteins. It reacts efficiently with primary amines under mild conditions to form stable amide bonds, making it valuable in the synthesis of bioconjugates for pharmaceutical and diagnostic applications. Commonly employed in the preparation of antibody-drug conjugates (ADCs) and labeled biomolecules due to its selective reactivity and compatibility with aqueous buffers. The presence of a protected hydr

Used as an activated ester in bioconjugation reactions, particularly in the modification of peptides and proteins. It reacts efficiently with primary amines under mild conditions to form stable amide bonds, making it valuable in the synthesis of bioconjugates for pharmaceutical and diagnostic applications. Commonly employed in the preparation of antibody-drug conjugates (ADCs) and labeled biomolecules due to its selective reactivity and compatibility with aqueous buffers. The presence of a protected hydrazine group allows for orthogonal functionalization, enabling sequential conjugation strategies in complex molecule assembly.

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